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3-(1-Naphthoyl)indole | 109555-87-5

3-(1-Naphthoyl)indole | 109555-87-5

CAS No. 109555-87-5 Chemical Name: 3-(1-Naphthoyl)indole Synonyms 3Naphthoylindole;-Naphthoyl Indole;3 Naphthoylindole;3-Naphthoylindole;1'-Naphthoyl Indole;3-(1-Naphthoyl)indole;3-(1-naphthylcarbonyl)indole;Ketone indol-3-yl 1-naphthyl;Indol-3-yl 1-Naphthyl Ketone;3- (1-Naphthoyl) Indole Powder CBNumber: CB52471302 Molecular Formula: C19H13NO Molecular Weight: 271.31 MDL Number: MFCD12923093 MOL File: 109555-87-5.mol MSDS File: SDS

Last updated: 2026-01-27 10:36:15

Product description

NumberPack SizePrice
1'-Naphthoyl Indole ≥98%116875mg$70
1'-Naphthoyl Indole ≥98%1168710mg$131
1'-Naphthoyl Indole ≥98%1168725mg$308
3-(1-Naphthoyl)indole N3680251g$120
3-(1-Naphthoyl)indole 95+%0902371g$152

3-(1-Naphthoyl)indole Properties

PropertyValue
Melting point236℃
Boiling point512.2±23.0 °C(Predicted)
Density1.267
storage temp.Sealed in dry,2-8°C
solubilityDMSO (Slightly), Methanol (Slightly)
formSolid
pka15.22±0.30(Predicted)
colorPale Orange to Light Pink
InChIInChI=1S/C19H13NO/c21-19(17-12-20-18-11-4-3-9-15(17)18)16-10-5-7-13-6-1-2-8-14(13)16/h1-12,20H
InChIKeyQIXQGVQLBPQVOR-UHFFFAOYSA-N
SMILESC(C1C2=C(NC=1)C=CC=C2)(C1=C2C(C=CC=C2)=CC=C1)=O
FDA UNII56CC3I2OAK

SAFETY

Risk and Safety Statements
ItemDetail
Symbol(GHS)GHS07
Signal wordWarning
Hazard statementsH302
Precautionary statementsP280-P305+P351+P338
NFPA 7040 2 0

3-(1-Naphthoyl)indole price

ManufacturerProduct numberProduct descriptionCAS numberPackagingPriceUpdated
Cayman Chemical116871'-Naphthoyl Indole ≥98%109555-87-55mg$702024-03-01
Cayman Chemical116871'-Naphthoyl Indole ≥98%109555-87-510mg$1312024-03-01
Cayman Chemical116871'-Naphthoyl Indole ≥98%109555-87-525mg$3082024-03-01
TRCN3680253-(1-Naphthoyl)indole109555-87-51g$1202021-12-16
Matrix Scientific0902373-(1-Naphthoyl)indole 95+%109555-87-51g$1522021-12-16

3-(1-Naphthoyl)indole Chemical Properties,Uses,Production

Description

3-(1-Naphthoyl)indole is a synthetic cannabinoid that is structurally similar to THC. It has been detected in human urine, plasma and autopsy samples by high-resolution mass spectrometry. It has been found to be hydroxylated into a number of metabolites including carboxy-3-(1-naphthoyl)indole, which may account for some of the psychoactive effects.

Chemical Properties

Off-White to Light Pink Solid.

Uses

Metabolite of JWH-018 (P283650).

Synthesis

To a cooled solution of indole (5.85g, 50mmol) in ether (50ml) under nitrogen was added slowly a solution of methylmagnesium bromide (3M) in ether (17.5ml). After addition, the reaction mixture was warmed up to room temperature and stirred for 2h at room temperature. Then, the mixture was cooled down again to 0°C and added slowly, stirring a solution of 1-naphthoylchloride (9.5g, 50mmol) in ether (50ml). The resulting mixture was warmed up to room temperature and stirred for 2h at room temperature, followed by a slow addition of saturated ammonium chloride solution (375ml). The mixture was then stirred overnight at room temperature. A white solid was formed, filtered, washed by ether, and dried under a high vacuum to give 3-(1-Naphthoyl)indole (12.3g, 91%).

3-(1-Naphthoyl)indole Preparation Products And Raw materials
Raw materials
  • Ethyl 1-naphthaleneacetate
  • 1-Naphthoyl chloride
  • Indole

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